10 results
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27ms
·
Sources: EU EUDAMED, US FDA
GE DETAX-OHMEDA ANESTHESIA DELIVERY UNIT (ADU)
FDA 510(k)
FDA Class 2
·Anesthesiology
Archimedes® Inflation Syringe
FDA UDI
Merit Medical Systems, Inc.·00884450202913·
CT LUCIA
FDA UDI
CARL ZEISS MEDITEC PRODUCTION, LLC·00843045100973·3-piece, monofocal, hydrophobic, acrylic, intra...
SIMPLICITY WINGED QD INFUSION SET
FDA 510(k)
FDA Class 2
·General Hospital
MEDTRONIC MINIMED PARADIGM INSULIN PUMP, MODELS MMT-515 AND MMT-715
FDA 510(k)
FDA Class 2
·General Hospital
Q2 MULTIPORT EXTENSION SET, 10 INCH
FDA Adverse Event
Malfunction
·QUEST MEDICAL, INC.·Product code FPA·June 7, 2016
ENSEAL G2 STRAIGHT JAW
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GEI·April 10, 2013
SECURE 3 MED/SURG BED
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·March 14, 2011
RIATA ACTIVE FIXATION
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·May 27, 2008
Inflation Kit. Label reads in part: ''CUSTOM KIT...MERIT MEDICAL''. Latex free, Sterile if package is unopened or undamaged. Part Numbers: K05-00122H, K05-50031D, K0510570, K05-01536A, K05-01153C, K05-00276C, K05-0019313, K05-00077F, K05-01296A, K05-00134D, K05-01676, K05-01250, K05-00800, K05-01545, K05-00819, K05-01069C, K05-00559F, K05-50078B, K05-00116C, K05-00459C, K05-01290A,K05-01146, K05-50054D, K05-00946B, K05-00203K, K05-00682B, K05-YSI008A, K05-YPI011, K05-00746, K05-003139, K05-00751G,K05-00180G, and K05-00553F.
FDA Recall
Terminated
·Merit Medical Systems, Inc·Product code DQO·October 1, 2003